EMA consults on heart failure medicine

Published: 14-Nov-2012

Trials might not adequately reflect impact of these drugs on patients


The European Medicines Agency (EMA) has launched a public consultation on revised guidance for pharmaceutical manufacturers developing acute heart failure drugs.

The changes reflect concern that trials might not adequately reflect the differing impact of these medicines on patients whose overall health and physical characteristics could vary widely.

EMA is inviting comments by 15 April 2013.

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